प्रस्तावित विषय : खोज निहित
Showing 1 - 20 results of 1,426 for search '"1332"', सवाल का समय: 2.04सेकंड परिणाम को परिष्कृत करें
  1. 1
    द्वारा Chen, Jing, Sun, Dalong, Liu, Mingli, Zhang, Shufan, Ren, Chuancheng
    प्रकाशित 2018
    “…This study aimed to examine the effectiveness of defibrinogen therapy on functional recovery and safety among 1332 consecutive ischemic stroke patients who had not received intravenous thrombolysis with recombinant tissue plasminogen activator. …”
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    Defibrinogen Therapy for Acute Ischemic Stroke: 1332 Consecutive Cases
  2. 2
    प्रकाशित 2022
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    Correction to Lancet Glob Health 2019; 7: e1332–45
  3. 3
    द्वारा Baird, S
    प्रकाशित 1983
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    Runs 1329 to 1332, 3.5 GeV/c Ring 2
  4. 4
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    P1332: ALL EMBRYONIC HEMATOPOIETIC WAVES EMERGE FROM HEMATO-ENDOTHELIAL PROGENITORS
  5. 5
    द्वारा Ravelli, A
    प्रकाशित 2013
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    PReS13-SPK-1332: Assessment of disease activity and damage in juvenile idiopathic arthritis
  6. 6
    द्वारा Rincic, Martina, Rados, Milan, Kopic, Janja, Krsnik, Zeljka, Liehr, Thomas
    प्रकाशित 2021
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    7p21.3 Together With a 12p13.32 Deletion in a Patient With Microcephaly—Does 12p13.32 Locus Possibly Comprises a Candidate Gene Region for Microcephaly?
  7. 7
    द्वारा Jafri, Farooqua, Fink, James, Higgins, Rodney R., Tervo, Raymond
    प्रकाशित 2011
    “…We report a rare occurrence of 22q13.3 duplication and 22q13.3 deletion in siblings, as a consequence of a mother's inversion on her 22nd chromosome (p13;q13.32). A 6 year old male was noted in infancy to have mild global developmental delay without dysmorphic features. …”
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    22q13.32 Deletion and Duplication and Inversion in the Same Family: A Rare Occurrence
  8. 8
    द्वारा Allyn, Paul, Schaenman, Joanna, Schwartz, Brian, Vijayan, Tara
    प्रकाशित 2018
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    1332. West Coast Transplant ID Conferences, A Model for Building Community in ID Disciplines?
  9. 9
    “…The ORFs of XYBX1332 and Oita-36 encode 3422 and 3425 amino acids, respectively. …”
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    Genetic diversity of the Yokose virus, XYBX1332, isolated from bats (Myotis daubentonii) in China
  10. 10
    द्वारा Rahimi, Zohreh, Mansouri Zaveleh, Omid, Rahimi, Ziba, Abbasi, Ardeshir
    प्रकाशित 2013
    “…Results: Analysis of AT2R -1332 G:A polymorphism indicated the absence of association between this polymorphism with T2DM and diabetic nephropathy. …”
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    AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
  11. 11
    द्वारा Sims, Matthew
    प्रकाशित 2019
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    1332. Identification of Genetic Markers Linked to Recurrent Methicillin-Resistant Staphylococcus aureus Skin and Soft-Tissue Infections
  12. 12
    “…We identified a novel duplication variant c.1332dup, p.(D445*) at exon 9 and a known silent variant c.1413A>G, p.(=), rs5930, NM_001195798.1 at exon 10 of the LDLR gene in both patients.…”
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    Identification of a novel nonsense variant c.1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia
  13. 13
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    Dynamic chromosomal tuning of a novel GAU1 lncing driver at chr12p13.32 accelerates tumorigenesis
  14. 14
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    1332 A Randomized, Double-Blind, Placebo-Controlled Trial of Trimethoprim-sulfamethoxazole vs. Placebo for Patients with an Incised and Drained Cutaneous Abscess
  15. 15
    द्वारा Trashorras Montecelos, Jesús
    पुस्तक
    Planificación de las instalaciones eléctricas en edificios de viviendas, industrias, oficinas y locales de pública concurrencia UF1332
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    “…Cytogenetic analysis revealed her karyotype to be 46,XX,r(22). aCGH identified a 180 kb 22q13.32 duplication, a de novo 2.024 Mb subtelomeric 22q13.32-q13.33 deletion, which is associated with Phelan-McDermid syndrome, and a maternal single gene 382-kb TUSC7 deletion of uncertain clinical significance located in the region of the 3q13.31 deletion syndrome. …”
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    Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22
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    1332. Single Dose Oral Amoxicillin Challenge is a Safe and Effective Strategy to Delabel Penicillin Allergies among Low Risk Hospitalized Children
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    “…Hereby, we presented a Chinese boy with a novel 4.36 Mb deletion at paternal 20q13.2-13.32, showing feeding difficulty, malnutrition, short stature, lower limb asymmetry, sightly abnormal facial appearance and mild intellectual abnormality. …”
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    Case Report: A Paternal 20q13.2-q13.32 Deletion Patient With Growth Retardation Improved by Growth Hormone
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    द्वारा Krushkal, Julia, Vural, Suleyman, Jensen, Travis L., Wright, George, Zhao, Yingdong
    प्रकाशित 2022
    “…Association of the increased copy number of the 20q11-q13.32 region with drug resistance may be complex and could involve multiple genes. …”
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    Increased copy number of imprinted genes in the chromosomal region 20q11-q13.32 is associated with resistance to antitumor agents in cancer cell lines
  20. 20
    “…CONCLUSION: Although the studied genetic variants were not associated with the risk of CHD, the 19q13.32 locus was associated with some of the cardiometabolic disorders in Algerian subjects.…”
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    Lack of association between genetic variants in the 19q13.32 region and CHD risk in the Algerian population: a population-based nested case-control study
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